Changes in erythropoiesis-stimulating agent (ESA) dosing and haemoglobin levels in US non-dialysis c

来源 :2013年中国肾性贫血治疗专家共识研讨会 | 被引量 : 0次 | 上传用户:liongliong421
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  Background.Recent clinical trials in cancer patients treated with erythropoiesis-stimulating agents (ESAs) and in CKD patients treated to haemoglobin (Hb) targets above the labeled range of 10-12 g/dL with ESAs raised safety concerns regarding ESA therapy.Subsequently, product labeling was revised including addition of a black-box warning and removal of many quality of life claims not supported by current standards, and there were changes in reimbursement and anaemia guidelines.The extent to which these events influenced ESA dosing and Hb levels in patients with chronic kidney disease not on dialysis (CKD-NOD) is not known.Methods.We used data collected in a series of crosssectional surveys between March 2005 and July 2009.Patients with CKD-NOD were selected from a random sample of free-standing US nephrology clinics.Information on demographics, insurance information, laboratory data and ESA use was abstracted from medical records by site investigators.We evaluated ESA treatment (use and dosing) and Hb levels over time and used multivariate linear regression to assess changes in ESA doses and Hb levels over time adjusting for case-mix differences.Results.Between 2005 and 2009, 15 836 CKD-NOD patients were sampled.During this period, ESA use declined from 60 to 46%, and the mean dose declined from 176 to 136 meg/month; the largest decline in use and in dose occurred beginning in 2007.Simultaneously, the mean (standard deviation) Hb level in ESA-treated patients declined from 11.5 (1.4) to 10.6 (1.2) g/dL, though the decline was most pronounced starting in 2007.As the mean Hb declined, the percent of treated patients with an Hb > 12 g/dL dropped from 27 to 12%, and the mean dose in this sub-population declined from 173 to 111 mcg/month.Conclusion.The emergence of safety concerns and the subsequent changes in product labeling, reimbursement and clinical practice guidelines all appear to have influenced physician dosing practices resulting in less frequent use of ESAs, lower ESA doses and lower achieved Hb levels in CKD-NOD patients.
其他文献
目的:探讨超氧化物歧化酶(SOD)检测在中枢神经系统白血病(CNSL)诊断中的意义.方法:收集2008年1月到2009年1月南方医院血液科30例中枢神经系统白血病患者脑脊液标本作为实验组,25例无中枢神经系统损害的急性白血病患者脑脊液标本作为对照组,采用黄嘌呤氧化酶法检测脑脊液SOD活性以及进行脑脊液脑脊液常规、生化及细胞涂片分析.结果:CNSL组脑脊液SOD活性显著高于对照组(P<0.05);C
目的:诱导耐药急性髓细胞白血病(AML)细胞凋亡是提高AML化疗疗效和改善预后的重要手段。本研究以耐阿霉素(ADM)的人AML多药耐药细胞株HL60/ADM为研究对象,研究IC20浓度雷公藤甲素能否提高化疗药物诱导耐药白血病细胞凋亡及其与Nrf2通路的关系。
会议
Farnesyltransferase inhibitors (FTIs) are currently under investigation for the treatment of leukemia.The mechanism of action of FTIs has not been clarified.In this study, we investigated the mechanis
目的:研究AML1-ETO融合基因阳性急性髓系白血病(acute myeloid leukemia,AML)患者c-kit突变的发生情况及临床意义。方法:采用PCR产物直接测序法检测31例AML1-ETO阳性AML患者c-kit基因17外显子突变的发生情况,并分析c-kit基因突变与患者的临床、实验室特征以及疗效的关系。
会议
目的:探讨外周血microRNA 101 (miR-101)表达水平在成人急性髓性白血病(Acute Myeloid Leukemia, AML)患者预后评估中的价值.方法:采用Real-time PCR法,检测初诊AML(非M3)患者及正常人外周血白细胞的microRNA 101水平,收集患者的临床特征和预后资料,统计分析它们之间的相关性.结果:初诊AML患者外周血的miR-101表达水平存在较
目的:研究分析髓系抗原(MyAg)表达在急性淋巴细胞白血病(Acute Lymphoblastic Leukemia, ALL)中的表达情况及其与预后的相关性.方法:选择中山大学附属中山医院2001年1月~2010年12月收治的初诊的成人急性淋巴细胞白血病病例共137例,所有患者均进行了骨髓细胞形态学、白血病免疫分型检查及Ph染色体检查,部分患者进行了分子生物学检测,分析髓系抗原在ALL中的表达情
目的:研究不同方案作为伴t(8; 21)急性髓系白血病缓解后的巩固治疗对疾病预后的影响。方法:回顾性分析多中心诊断的诱导缓解后接受≥2疗程巩固治疗的111例伴t(8; 21) AML患者的临床资料,分析不同巩固方案对OS和PFS的影响。结果:(1) 111例患者[男:女=65:46,中位年龄25(2-60)岁]中接受常规方案巩固化疗者(A组)有36例,含DAE、<4程MiDAC、<3程HiDAC强
目的:探讨利妥昔单抗对弥漫大B细胞淋巴瘤患者Th17细胞及相关细胞因子体外的影响及其意义。方法:DLBCL初治患者和体检健康者各20例,每个对象分别采集4份外周血标本,分离外周血单个核细胞(PBMCs),按照培养条件的不同分成4个亚组:空白组(A亚组)、加入利妥昔单抗组(B亚组)、加入利妥昔单抗和血清组(C亚组)和极化组(D亚组)(加IL-6和TGF-β)。
背景和目的:多发性骨髓瘤患者RANKL表达异常增高使RANKL/RANK信号系统过度激活,导致破骨细胞(Osteoclast,oC)大量生成且功能亢进在骨髓瘤骨病(Myeloma bone disease,MBD)的发生、发展中起关键作用,因此抑制RANKL/RANK信号转导途径从而抑制OC的形成及其破骨功能是治疗MBD有效方法之一。前期研究发现RANK蛋白上存在一个新基序:IVVY,介导了一条O
会议
背景反复输血或使用红细胞生成刺激剂(ESA)都可以用于治疗肾性贫血.但是对两种治疗方法的选择,应该针对患者的实际情况,根据两种治疗方法的相对利弊进行选择.单纯的Hb降低不作为输血的理由,不能为了Hb达标而输血.慢性贫血患者输血是为了防止组织缺氧或心力衰竭.在ESA治疗Hb达标的患者,仅在急性失血(如急性出血、急性溶血、严重炎症或外科血液丢失)时输血.输血患者患急性冠脉综合征时有更高的死亡率.使用输
会议